Senior Statistical Programmer (FSP), South Africa
South Africa, Remote Job ID R0000030887 Category Statistical Programming Date Posted 01/30/2025Overview
As a member of Parexel’s Statistical Programming group, you analyze, summarize, and graphically present clinical data to assess the safety and efficacy of the clinical trial. It requires attention to detail, a commitment to quality, and effective communication to ensure new treatments reach patients faster. You will work in different therapeutic areas assessing a variety of data entries and endpoints in an ever-changing environment. We provide a fertile environment for growth, with extensive training, mentoring, and technical knowledge sharing.
You will work closely with the client and Parexel teams and collaborate to maximize the collective strength. Experience a supportive and motivating work environment where our teams offer an inherent breadth of knowledge within a diverse and inclusive workplace.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Analytical
- Detail-oriented
- Independent
- Proactive
- Responsible
- Team-player
About This Role
Parexel is currently seeking a Senior Statistical Programmer to join us in South Africa, dedicated to a single sponsor.
Picture Yourself At Parexel:
The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data.
What You'll Do At Parexel:
• Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs.
• Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis.
• Support the electronic submission preparation and review.
• Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities.
• Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers.
• Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices.
• Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors.
• Independently leads and / or performs programming assignments with minimal supervision.
• Support improvement initiatives.
Role Requirements:
• Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required.
• Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development.
• Demonstrated proficiency in analytical programming.
• Have in-depth understanding of clinical data structure (e.g., CDISC standards) and relational database.
• Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21.
• Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.
• Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.
• Have good understanding of regulatory, industry, and technology standards and requirements.
• Have good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs.
• Demonstrated ability to work in a team environment with clinical team members.
Additional Requirements:
• Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings.
• Knowledge of the drug development process, clinical trial methodology, statistics, and familiarity with global regulatory requirements.
• Experience in other software packages (e.g., R)
• Experience with the Linux operating system.
A little about us:
Highly qualified and dynamic team. Multinational working environment. Smooth induction and training program. We offer competitive financial packages, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
Parexel has a fully flexible work arrangement - you can be fully home based. But if you live close to our office and you want to use it, you are always welcome, and we will keep the desk ready for you!
#LI-REMOTE
Potential Career Path
Parexel offers career paths for Statistical Programmers to progress in their technical position or managerial position, as well as options to move to other areas of the business.
- Statistical Programmer I
- Statistical Programmer II
- Senior Statistical Programmer
- Subject Matter ExpertPeople Management
Employee Insights
Why Statistical Programmers work at Parexel
